At a Glance
- Tasks: Lead clinical programming activities and ensure quality data management for impactful clinical trials.
- Company: Join a leading organisation in biostatistics and data analytics.
- Benefits: Competitive salary, flexible working options, and opportunities for professional growth.
- Other info: Dynamic team environment with a focus on innovation and continuous improvement.
- Why this job: Make a difference in healthcare by transforming data into actionable insights.
- Qualifications: Experience in clinical programming and strong analytical skills required.
The predicted salary is between 45000 - 55000 £ per year.
The Experienced Clinical Programmer is an experienced clinical trial programmer with in-depth knowledge in industry standard and complex data structures, programming languages, and/or reporting solutions with proven technical capabilities in leading clinical trial activities and/or teams in accordance with departmental processes and procedures.
The position is responsible for oversight or the development of one or more clinical data management trial activities of moderate to high complexity/criticality. This includes data model specifications, data stream integrations and transformation of source to internal data models and/or CDISC submission ready SDTM tabulation packages (aCRF, define.xml, cSDRG, etc). The role involves creating and executing edit check programs, listings and report solutions to aid in monitoring of safety, risk, compliance and ensures quality data review.
Responsibilities include:
- Accountable for one or more clinical programming trial activities of moderate to high complexity, scope and/or criticality.
- Performing comprehensive review of, and providing input into, project requirements and documentation.
- Identifying gaps, proposing solutions and applying expertise to improve efficiency of programming tasks and/or improve overall quality of programming deliverables.
- Ensuring latest standards are being utilized, current technologies are deployed.
- Creating and/or reviewing specifications for mapping internal data review model for fit for purpose reporting and/or as well as submission ready CDISC SDTM.
- Designing mapping algorithms for nonstandard conversions.
- Responsible for creation or review of internal data model for fit for purpose reporting consumption and/or submission ready CDISC SDTM packages for health authority submissions and keeping abreast in changing regulatory requirements.
- Programming, or oversight of quality review checks, study specific reports for use by team members and consumers of data.
- Supporting and/or leading in developing and implementing process, system and tool improvement initiatives within compliance with departmental processes and procedures.
Required Skills:
- Advanced Analytics
- Analytical Reasoning
- Biological Sciences
- Biostatistics
- Clinical Trials
- Data Modeling
- Data Privacy Standards
- Data Quality
- Data Savvy
- Detail-Oriented
- Good Clinical Practice (GCP)
- Report Writing
- Research Ethics
- Researching
- Statistical Analysis Systems (SAS) Programming
- Statistics
- Technologically Savvy
Preferred Skills:
- Advanced Analytics
- Analytical Reasoning
- Biological Sciences
- Biostatistics
- Clinical Trials
- Data Modeling
- Data Privacy Standards
- Data Quality
- Data Savvy
- Detail-Oriented
- Good Clinical Practice (GCP)
- Report Writing
- Research Ethics
- Researching
- Statistical Analysis Systems (SAS) Programming
- Statistics
- Technologically Savvy
Experienced Clin Programmer employer: 7360-Janssen-Cilag Limited Legal Entity
Join a leading organisation in High Wycombe, where we prioritise innovation and excellence in clinical programming. Our collaborative work culture fosters professional growth, offering extensive training and development opportunities to enhance your skills in biostatistics and data analytics. With a commitment to quality and compliance, we provide a supportive environment that empowers you to make a meaningful impact in the field of clinical trials.
Contact Details:
7360-Janssen-Cilag Limited Legal Entity Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Experienced Clin Programmer
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant meetups, and engage on platforms like LinkedIn. We all know that sometimes it’s not just what you know, but who you know that can help you land that dream job.
✨Tip Number 2
Prepare for interviews by practising common questions and scenarios related to clinical programming. We recommend doing mock interviews with friends or mentors to boost your confidence and refine your answers.
✨Tip Number 3
Showcase your skills through a portfolio! If you’ve worked on any projects or have examples of your programming work, compile them into a neat presentation. This gives potential employers a tangible sense of what you can do.
✨Tip Number 4
Don’t forget to apply through our website! We’re always on the lookout for talented individuals like you. Plus, it’s a great way to ensure your application gets the attention it deserves.
We think you need these skills to ace Experienced Clin Programmer
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Experienced Clinical Programmer role. Highlight your experience with clinical trials, data management, and programming languages. We want to see how your skills match what we're looking for!
Showcase Your Projects:Include specific examples of projects you've worked on that demonstrate your expertise in data modelling and reporting solutions. We love seeing real-world applications of your skills, so don’t hold back!
Be Clear and Concise:When writing your application, keep it clear and concise. Use bullet points where possible to make it easy for us to read through your qualifications and experiences. We appreciate a straightforward approach!
Apply Through Our Website:Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. We can’t wait to see what you bring to the table!
How to prepare for a job interview at 7360-Janssen-Cilag Limited Legal Entity
✨Know Your Data Inside Out
Make sure you brush up on your knowledge of data structures and programming languages relevant to clinical trials. Be prepared to discuss specific examples of how you've used these skills in past projects, as this will show your depth of understanding and experience.
✨Showcase Your Problem-Solving Skills
During the interview, be ready to talk about challenges you've faced in clinical programming and how you overcame them. Highlight your analytical reasoning and detail-oriented approach, as these are crucial for identifying gaps and proposing effective solutions.
✨Familiarise Yourself with CDISC Standards
Since the role involves creating submission-ready CDISC SDTM packages, make sure you're well-versed in these standards. Discuss any previous experience you have with mapping algorithms or data model specifications to demonstrate your capability in this area.
✨Prepare Questions About Process Improvements
Think about how you can contribute to process, system, and tool improvements within the team. Prepare insightful questions that show your interest in enhancing efficiency and quality in programming tasks, which will reflect your proactive mindset.
